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Technician; Quality

Online/Remoto - Ideal para candidatos en
08740, Sant Andreu de la Barca, Cataluna, España
Empresa: Amaris Consulting
Remoto/Desde casa posición
Publicado en 2026-02-01
Especializaciones laborales:
  • Control de Calidad
    Ingeniería de Calidad, Especialista de Gestión de Calidad
Descripción del trabajo
Puesto: Technician (Quality)
Location: Sant Andreu de la Barca

Take your career to the next level with Amaris Consulting as a Validation & Qualification Technician.  Be part of an international team, thrive in a global group with a €800M turnover and over 1,000 clients worldwide, and an agile environment.

✍️  WHAT WOULD YOU NEED? ✍️
~2+ years of hands-on experience in  Quality Assurance  within the pharmaceutical or life sciences industry.
~ Proven experience in  equipment and room qualification  and  manufacturing process validation  .
~ Strong skills in  GMP-compliant documentation management  and IT system validation (e.g., Track Wise or similar).
~ Degree in  Chemical, Industrial, or Pharmaceutical Engineering  or related scientific disciplines; postgraduate training in Quality Systems, Validation, or GMP is a strong plus.
~ Solid understanding of  GMP regulations  and pharmaceutical quality systems.
~ Experience working in  manufacturing plants  , interacting with technical and operational teams.
~ High level of  autonomy, attention to detail, and regulatory compliance focus  .
~ Ability to work effectively with  cross-functional teams  (QA, Production, QC, Engineering, Procurement).
~ Fluent English  and  Spanish  ;  German  is a nice-to-have.
~ Based in  Sant Andreu de la Barca  , hybrid work mode (approx. 60% on-site, 40% remote).

&##128073;  WHAT WILL YOU BE DOING?
Execute  equipment, room, and facility qualification activities  according to GMP standards.
Support  manufacturing process validation  and implementation or modification of production lines.
Provide support in  IT system validation  , including Quality Management Systems, in coordination with the Quality Systems team.
Prepare, review, and execute  GMP-compliant validation and qualification documentation  .
Coordinate validation activities with internal departments and, when required, external suppliers.
Participate in internal audits, supplier audits, and regulatory readiness activities.
Support acquisition or integration of new production lines, including space allocation, qualification strategy, and execution.
Work autonomously within  multidisciplinary teams  , ensuring timely delivery and high-quality outcomes.
Quickly adapt to ongoing activities and contribute actively to operational continuity without heavy supervision.

&##128640;

WHY US?&##128640;?
Join our dynamic team of talented people and discover a world full of growth and opportunity. Here's what we offer:
Rapid growth through a personalised career path and salary assessment. 70% of our senior leaders started in entry-level positions.
Improve your skills through our Technology Academy catalogue, Udemy platform, language classes, webinars and workshops.
Take control of your training with a personal annual budget and company-paid certifications.
Enjoy flexible policies, remote work options and excellent social benefits such as transport and restaurant tickets, childcare support and private health insurance.
Benefit from our WeCare programme, which supports employees in critical situations.
Unlock your full potential, both professionally and personally.

Amaris Consulting prides itself on being an equal opportunity employer. We are committed to promoting diversity within the workforce and creating an inclusive work environment. To this end, we welcome applications from all qualified candidates, regardless of gender, sexual orientation, race, ethnicity, creed, age, marital status, disability or other characteristics.
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